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SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide Popular
  • SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide

  • Exam (elaborations) • 356 pages • 2023
  • SOCRA EXAM PREP | 2023 Update | Questions and Verified Answers| Highly Rated Guide Q: What 4 aspects of a trial should a sponsor focus on when monitoring for compliance per 21 CFR 312.56? Answer: 1) Progress of investigations under IND 2) Secure compliance or discontinue investigators that are not compliant and notify FDA 3) Review safety/effectiveness of drug and report safety issues to FDA + make annual reports or progress 4) Notify FDA, all IRBs and all investigators if drug presen...
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SOCRA UPDATED Exam Questions and  CORRECT Answers
  • SOCRA UPDATED Exam Questions and CORRECT Answers

  • Exam (elaborations) • 13 pages • 2024
  • Which of the following is a disclosure of financial interests form? - FDA Form 3455 Which of the following is a certification of financial interest form? - FDA Form 3454 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: - FDA Form 3455 This form is submitted by sponsor to the FDA prior to the beginning of the drug trial - Investigational New Drug Application (1571) In the top right corner, form have OMB number. What does it stand ...
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SOCRA TOP Exam Guide Questions and  CORRECT Answers
  • SOCRA TOP Exam Guide Questions and CORRECT Answers

  • Exam (elaborations) • 25 pages • 2024
  • When isn't an IND application needed? - IND Application is not needed if investigation does not support change in labeling. What information must the general IND include? (21 CFR Part 312.23) - -FDA Form 1571 -FDA Form 1571 cover sheet -Table of contents -Investigative Plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/Toxicology -Previous human research/literature information -Additional information (drug dependence and abuse potential)
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SOCRA PASSED Exam Questions and  CORRECT Answers
  • SOCRA PASSED Exam Questions and CORRECT Answers

  • Exam (elaborations) • 16 pages • 2024
  • Respect for persons, justice, beneficence - List the three ethical principles of the Belmont report Experiment that involves a test article and one or more human subjects - does not include experiments which are nonclinical lab studies - Define clinical investigation Someone who is or becomes A participate in research either as a recipient of the test article or as a control - Human subject is: Life threatening circumstances deem use of test article necessary, inability to communicate o...
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SOCRA (CCRP) Exam Practice  Questions and Answers 2024
  • SOCRA (CCRP) Exam Practice Questions and Answers 2024

  • Exam (elaborations) • 2 pages • 2024
  • The Belmont Report's principle of respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that: - CORRECT AND ANSWER-Persons with diminished autonomy are entitled to protection. Which of the following is an example of how the principle of beneficence can be applied to a study employing human subjects? - CORRECT AND ANSWER-Determining that the study has a maximization of benefits and a minimization ...
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SOCRA Practice Test Certification Final Exam Questions with 100% Correct  answers
  • SOCRA Practice Test Certification Final Exam Questions with 100% Correct answers

  • Exam (elaborations) • 10 pages • 2024
  • Which of the following is a disclosure of financial interests form? - CORRECT ANSWER-FDA Form 3455 Which of the following is a certification of financial interest form? - CORRECT ANSWER-FDA Form 3454 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: - CORRECT ANSWER-FDA Form 3455 This form is submitted by sponsor to the FDA prior to the beginning of the drug trial - CORRECT ANSWER-Investigational New Drug Application (1571) In...
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Socra Exam Prep Test 2024- with 100% Correct Answers ( A Graded)
  • Socra Exam Prep Test 2024- with 100% Correct Answers ( A Graded)

  • Exam (elaborations) • 25 pages • 2024
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  • Laws - ANSWER passed by national legislative bodies; establish authority of national regulatory body Regulations - ANSWER Passed by regulatory authorities; controls how medical products are investigated and approved; have effect of law guidance - ANSWER "current thinking" of regulatory bodies; non-binding ICH - ANSWER Developed to keep people doing things the same way across the world; international effort to harmonize the technical requirements for product registration
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SOCRA EXAM 2024- with 100% Correct Answers ( A Graded)
  • SOCRA EXAM 2024- with 100% Correct Answers ( A Graded)

  • Exam (elaborations) • 50 pages • 2024
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  • SOCRA EXAM 2024- with 100% Correct Answers ( A Graded) Electronic signature are currently accepted for any and all records, paper or electronic form. True or False? - ANSWER False. The general provisions for electeonic signature criteria apply to records that are i. Created, modified, maintained, archived, retrieved, or transmitted, in electronic form ii. The criteria do not apply to paper records that are or have been transmitted by electronic means. If the electronic records meet the c...
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SOCRA Practice Test - with 100% Correct Answers ( A Guaranteed)
  • SOCRA Practice Test - with 100% Correct Answers ( A Guaranteed)

  • Exam (elaborations) • 14 pages • 2024
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  • Which of the following is a disclosure of financial interests form? - ANSWER FDA Form 3455 Which of the following is a certification of financial interest form? - ANSWER FDA Form 3454 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: - ANSWER FDA Form 3455 This form is submitted by sponsor to the FDA prior to the beginning of the drug trial - ANSWER Investigational New Drug Application (1571)
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Socra CCRP Exam Prep Test 2024- with 100% Correct Answers ( A Graded)
  • Socra CCRP Exam Prep Test 2024- with 100% Correct Answers ( A Graded)

  • Exam (elaborations) • 6 pages • 2024
  • Available in package deal
  • Contract Research Organization - ANSWER A person or an organization (commercial, academic, or other) contracted by the sponsor to perform one or more of a sponsor's trial-related duties and functions. When a short form is used for informed consent the witness must sign the short form or the summary? - ANSWER False-they must sign both What is FDA form 3454 - ANSWER Certification Financial Interests and Arrangements of Clinical Investigators
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